HGVS | Genome Assembly |
---|---|
NC_000010.11:g.78033895C= , CM000672.2:g.78033895C= | GRCh38 |
NC_000010.10:g.79793653C= , CM000672.1:g.79793653C= | GRCh37 |
NC_000010.9:g.79463659C= | NCBI36 |
NG_012633.1:g.5136C= | |
NG_029648.1:g.646G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360830.9:c.-7C= | ENSP00000354074.5:n.-7C= | |
ENST00000372360.9:c.-7C= MANE Select | ENSP00000361435.4:n.-7C= | |
ENST00000440692.6:c.-7C= | ENSP00000414321.1:n.-7C= | |
ENST00000464716.6:c.-7C= | ENSP00000494231.1:n.-7C= | |
ENST00000465692.2:n.5C= | ||
ENST00000466129.6:n.10C= | ||
ENST00000476545.6:c.-7C= | ENSP00000494169.1:n.-7C= | |
ENST00000478655.6:n.33C= | ||
ENST00000485708.7:n.33C= | ||
ENST00000613865.5:c.-7C= | ENSP00000478869.2:n.-7C= | |
ENST00000645440.1:c.-7C= | ENSP00000496738.1:n.-7C= | |
ENST00000645698.1:n.22C= | ||
ENST00000360830.8:c.-7C= | ENSP00000354074.4:n.-7C= | |
ENST00000372360.7:c.-7C= | ENSP00000361435.3:n.-7C= | |
ENST00000435275.5:c.-7C= | ENSP00000415549.1:n.-7C= | |
ENST00000440692.5:c.-7C= | ENSP00000414321.1:n.-7C= | |
ENST00000464716.5:n.22C= | ||
ENST00000466129.5:n.10C= | ||
ENST00000476545.5:n.18C= | ||
ENST00000478655.5:n.33C= | ||
ENST00000485708.6:n.52C= | ||
ENST00000613865.4:c.-7C= | ENSP00000478869.1:n.-7C= | |
NM_001026.4:c.-7C= | NP_001017.1:n.-7C= | |
NM_001142282.1:c.-7C= | NP_001135754.1:n.-7C= | |
NM_001142283.1:c.-7C= | NP_001135755.1:n.-7C= | |
NM_001142284.1:c.-7C= | NP_001135756.1:n.-7C= | |
NM_001142285.1:c.-7C= | NP_001135757.1:n.-7C= | |
NM_033022.3:c.-7C= | NP_148982.1:n.-7C= | |
NM_001142285.2:c.-7C= | NP_001135757.1:n.-7C= | |
NM_033022.4:c.-7C= MANE Select | NP_148982.1:n.-7C= | |
NM_001026.5:c.-7C= | NP_001017.1:n.-7C= | |
NM_001142282.2:c.-7C= | NP_001135754.1:n.-7C= | |
NM_001142283.2:c.-7C= | NP_001135755.1:n.-7C= | |
NM_001142284.2:c.-7C= | NP_001135756.1:n.-7C= |